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Are substitutions in the first hypervariable region of the mitochondrial DNA displacement-loop in sudden infant death syndrome due to maternal inheritance?
Arnestad M, Opdal SH, Musse MA, Vege A, Rognum TO. Arnestad M, et al. Among authors: rognum to. Acta Paediatr. 2002;91(10):1060-4. doi: 10.1080/080352502760311557. Acta Paediatr. 2002. PMID: 12434891
AIM: To investigate whether all substitutions in the first hypervariable region (HVR1) in sudden infant death syndrome (SIDS) can be recovered along the maternal line of the family (inherited), or whether SIDS victims have new substitutions compared to maternal rela …
AIM: To investigate whether all substitutions in the first hypervariable region (HVR1) in sudden infant death syndrome (SIDS) can be …
Mitochondrial microsatellite instability in colorectal carcinomas--frequency and association with nuclear microsatellite instability.
Guleng G, Løvig T, Meling GI, Andersen SN, Rognum TO. Guleng G, et al. Among authors: rognum to. Cancer Lett. 2005 Feb 28;219(1):97-103. doi: 10.1016/j.canlet.2004.07.018. Cancer Lett. 2005. PMID: 15694669
D310 alterations were found in 32 (34%) of the carcinomas, in contrast to two persons (2%) in the control group. Thus, when frequency is concerned, D310 seems to be a hotspot for alterations in colorectal cancer. ...
D310 alterations were found in 32 (34%) of the carcinomas, in contrast to two persons (2%) in the control group. Thus, when frequency …
[Bed sharing and sudden infant death].
Stray-Pedersen A, Arnestad M, Vege A, Sveum L, Rognum TO. Stray-Pedersen A, et al. Among authors: rognum to. Tidsskr Nor Laegeforen. 2005 Nov 3;125(21):2919-21. Tidsskr Nor Laegeforen. 2005. PMID: 16276370 Norwegian.
BACKGROUND: The aim of the study was to investigate bed sharing as a risk factor for sudden infant death syndrome (SIDS). MATERIAL AND METHODS: Firstly, SIDS cases examined at our institute in two six-year periods before and after the back-to-sleep campaign (1984-89 …
BACKGROUND: The aim of the study was to investigate bed sharing as a risk factor for sudden infant death syndrome (SIDS). MATERIAL AN …
Helicobacter pylori antigen in stool is associated with SIDS and sudden infant deaths due to infectious disease.
Stray-Pedersen A, Vege A, Rognum TO. Stray-Pedersen A, et al. Among authors: rognum to. Pediatr Res. 2008 Oct;64(4):405-10. doi: 10.1203/PDR.0b013e31818095f7. Pediatr Res. 2008. PMID: 18535491

H. pylori antigen was detected in 8% (12/156) of the live controls compared with 25% (30/122) of SIDS cases (p < 0.001), 53% (9/17) of deaths due to infection (p < 0.001), and 9% (1/11) of accidental/violent deaths (p = 0.60). ...Detection of H. pylori antigen in sto

H. pylori antigen was detected in 8% (12/156) of the live controls compared with 25% (30/122) of SIDS cases (p < 0.001), 53% (9/17) of de

Polymorphisms in the myeloid differentiation primary response 88 pathway do not explain low expression levels in sudden infant death syndrome.
Bjørnvall CD, Opdal SH, Rognum TO, Ferrante L. Bjørnvall CD, et al. Among authors: rognum to. Acta Paediatr. 2019 Jul;108(7):1262-1266. doi: 10.1111/apa.14696. Epub 2018 Dec 26. Acta Paediatr. 2019. PMID: 30550627
Gene variants predisposing to SIDS: current knowledge.
Opdal SH, Rognum TO. Opdal SH, et al. Among authors: rognum to. Forensic Sci Med Pathol. 2011 Mar;7(1):26-36. doi: 10.1007/s12024-010-9182-9. Epub 2010 Jul 11. Forensic Sci Med Pathol. 2011. PMID: 20623341 Review.
Most likely genetic predisposition to SIDS represent a polygenic inheritance pattern leading to sudden death when combined with other risk factors, such as a vulnerable developmental stage of the central nervous system and/or the immune system, in addition to
Most likely genetic predisposition to SIDS represent a polygenic inheritance pattern leading to sudden death when combined wit …
Altered gene expression and possible immunodeficiency in cases of sudden infant death syndrome.
Ferrante L, Rognum TO, Vege Å, Nygård S, Opdal SH. Ferrante L, et al. Among authors: rognum to. Pediatr Res. 2016 Jul;80(1):77-84. doi: 10.1038/pr.2016.45. Epub 2016 Mar 9. Pediatr Res. 2016. PMID: 26959483
The purpose of this study was to investigate mRNA gene expression in SIDS cases and controls, in order to uncover genes that are differentially expressed in the two groups. ...RESULTS: Seventeen genes showed significantly altered expression compared to contro …
The purpose of this study was to investigate mRNA gene expression in SIDS cases and controls, in order to uncover genes that a …
Is there any correlation between HLA-DR expression in laryngeal mucosa and interleukin gene variation in sudden infant death syndrome?
Ferrante L, Opdal SH, Vege A, Rognum TO. Ferrante L, et al. Among authors: rognum to. Acta Paediatr. 2013 Mar;102(3):308-13. doi: 10.1111/apa.12107. Epub 2012 Dec 27. Acta Paediatr. 2013. PMID: 23186119
Our aim was to search for a possible association between cytokine polymorphisms and immune stimulation of the laryngeal mucosal in SIDS. ...The findings were related to cytokine gene polymorphisms as well as to the level of various cytokines in the cerebrospi …
Our aim was to search for a possible association between cytokine polymorphisms and immune stimulation of the laryngeal mucosal in SI …
Aquaporin-4 gene variation and sudden infant death syndrome.
Opdal SH, Vege A, Stray-Pedersen A, Rognum TO. Opdal SH, et al. Among authors: rognum to. Pediatr Res. 2010 Jul;68(1):48-51. doi: 10.1203/PDR.0b013e3181df4e7c. Pediatr Res. 2010. PMID: 20351659
The purpose of this study was to investigate the aquaporin-4 (AQP4) gene in cases of sudden infant death syndrome (SIDS) and controls and to elucidate the hypothesis that a genetically determined disturbed water homeostasis in the brain is involved as a predisposing …
The purpose of this study was to investigate the aquaporin-4 (AQP4) gene in cases of sudden infant death syndrome (SIDS) and controls …
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